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"Baker Seaver" liquid drug applicator (unsterilized) - Taiwan Registration 823093d228de02dc8cd52d02395cb172

Access comprehensive regulatory information for "Baker Seaver" liquid drug applicator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 823093d228de02dc8cd52d02395cb172 and manufactured by ALLY HOSPITAL SUPPLY CO., LTD.. The authorized representative in Taiwan is BECQUEREL & SIEVERT CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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823093d228de02dc8cd52d02395cb172
Registration Details
Taiwan FDA Registration: 823093d228de02dc8cd52d02395cb172
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Device Details

"Baker Seaver" liquid drug applicator (unsterilized)
TW: "่ฒๅ…‹่ฅฟๅผ—" ๆถฒ้ซ”่—ฅ็‰ฉ็ตฆ่—ฅๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

823093d228de02dc8cd52d02395cb172

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Liquid Drug Dispenser (J.6430)".

J General hospital and personal use equipment

J.6430 ๆถฒ้ซ”่—ฅ็‰ฉ็ตฆ่—ฅๅ™จ

Domestic;; Contract manufacturing

Dates and Status

Apr 02, 2014

Apr 02, 2019

Sep 12, 2018

Cancellation Information

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